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Maxi-probe Irrigation Needle MAXP234

by Tulsa Dental Products LLC

Maxi-probe Irrigation Needle MAXP234 is a Class I device made by Tulsa Dental Products LLC, listed in FDA GUDID since 17 Aug 2022 (UDI-DI D716MAXP2341), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD716MAXP2341 UDI-DI Date17 Aug 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Maxi-probe Irrigation Needle
Generic name
Dental syringe needle, single-use
Model / Ref / Catalog
MAXP234
Primary DI / UDI-DI
D716MAXP2341
FDA product code
EIC
GMDN term
Dental syringe needle, single-use
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental syringe needle, single-use

Other devices from Tulsa Dental Products LLC

See all devices from Tulsa Dental Products LLC →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)